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HRID 14998作成日:2026年10月23日

Iodide Ion → 3-(4,4-difluorocyclohexyl)-2-(5,5-dioxo-5,10-dihydrophenothiazin-2-yl)-N-(5-methoxythiazolo[5,4-b]pyridin-2-yl)propionamide

https://huagongshe.com/ja/reaction/14998

反応式

関与物質

役割名称HCID仕込み量
反応物Iodide IonHCID 30165—
反応物Ethyl-4,4-difluorocyclohexane carboxylateHCID 2779138—
反応物5-Methoxy[1,3]thiazolo[5,4-b]pyridin-2-amineHCID 2801557—
反応物tert-butyl 2-ethoxycarbonylmethyl-5,5-dioxo-5H-phenothiazine-10-carboxylateHCID 59340981—
反応物1,1-Difluoro-4-(iodomethyl)cyclohexaneHCID 67236985—
生成物3-(4,4-difluorocyclohexyl)-2-(5,5-dioxo-5,10-dihydrophenothiazin-2-yl)-N-(5-methoxythiazolo[5,4-b]pyridin-2-yl)propionamideHCID 58024254—

反応手順

Analogously to Example 36 and Example 44, tert-butyl 2-ethoxycarbonylmethyl-5,5-dioxo-5H-phenothiazine-10-carboxylate, 1,1-difluoro-4-iodomethylcyclohexane (prepared from commercially available ethyl 4,4-difluorocyclohexanecarboxylate analogously to the synthesis of the iodide described in Example 40) and 5-methoxy-thiazolo[5,4-b]pyridin-2-ylamine give 3-(4,4-difluorocyclohexyl)-2-(5,5-dioxo-5,10-dihydrophenothiazin-2-yl)-N-(5-methoxythiazolo[5,4-b]pyridin-2-yl)propionamide.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732440B2
出典データセットuspto-grants-2010_06
ORD IDord-3958a078b667471db485796a4948a9a2
出典メモuspto-grants-2010_06